A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689621



Internal ID21211475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10587046..10587246hg38UCSC Ensembl
chr2:10727172..10727372hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804676
Supporting Variants
Samples
Known GenesNOL10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689621
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.28125


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